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July 08, 2003; 61 (1) Brief Communications

Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP

H.R. Morris, Y. Osaki, J. Holton, A.J. Lees, N.W. Wood, T. Revesz, N. Quinn
First published July 8, 2003, DOI: https://doi.org/10.1212/01.WNL.0000072325.27824.A5
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Article Information

vol. 61 no. 1 102-104
DOI: 
https://doi.org/10.1212/01.WNL.0000072325.27824.A5
PubMed: 
12847166
Published By: 
Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology
Print ISSN: 
0028-3878
Online ISSN: 
1526-632X
History: 
  • Received April 26, 2002
  • Accepted March 1, 2003
  • First Published July 8, 2003.
Copyright & Usage: 
© 2003

Author Disclosures

    1. H.R. Morris, MRCP PhD,
    2. Y. Osaki, MD,
    3. J. Holton, MD,
    4. A.J. Lees, MD,
    5. N.W. Wood, PhD,
    6. T. Revesz, MD and
    7. N. Quinn, MD
  1. H.R. Morris, MRCP PhD,
  2. Y. Osaki, MD,
  3. J. Holton, MD,
  4. A.J. Lees, MD,
  5. N.W. Wood, PhD,
  6. T. Revesz, MD and
  7. N. Quinn, MD
  1. From the National Hospital for Neurology and Neurosurgery (Dr. Morris), Queen Square, London; Department of Medicine and Geriatrics (Dr. Osaki), Kohasu, Oko-cho, Nankoku, Japan; Sara Koe PSP Research Centre, Queen Square Brain Bank for Neurological Disorders (Drs. Holton, Lees, and Revesz), Department of Molecular Pathogenesis (Drs. Morris, Holton, Lees, Wood, and Revesz), and Sobell Department of Motor Neuroscience and Movement Disorders (Dr. Quinn), Institute of Neurology, Queen Square, London; and Reta Lila Weston Institute of Neurological Sciences (Dr. Lees), Windeyer Building, University College London, UK.
  1. Address correspondence and reprint requests to Prof. N. Quinn, Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, Queen Square, London WC1N 3BG, UK; e-mail: n.quinn{at}ion.ucl.ac.uk

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